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NCT06839105
A Clinical Study to Evaluate the Safety and Tolerability of AWT020 in Patients With Advanced Malignancies
The purpose of this phase I clinical study was to evaluate the safety and tolerability of AWT020 monotherapy and combination with other antitumor therapies in patients with advanced malignancies
Trial Details
NCT ID NCT06839105
Phase PHASE1
Sponsor Shanghai Junshi Bioscience Co., Ltd.
Status RECRUITING
Cancer Type Adenocarcinoma Lung Cancer
Interventions Taxol Cisplatin or Carboplatin Pemetrexed Oxaliplatin Capecitabine Bevacizumab
Locations (sample) Fuzhou, Fujian, China|26.06139,119.30611 Guangzhou, Guangdong, China|23.11667,113.25 Harbin, Heilongjiang, China|45.75,126.65 Luoyang, Henan, China|34.67345,112.43684 Wuhan, Hubei, China|30.58333,114.26667
Key Eligibility Criteria
Both male and female subjects who are at least 18 years old at the time of signing the consent form; Inclusion of patients with advanced malignancies confirmed histologically or cytologically and meeting the following requirements: Single-agent dose escalation and expansion phase to include patients with advanced malignant tumors who have failed or are intolerant of standard t… Therapeutic effect expansion stage of single drug:
For full eligibility, visit ClinicalTrials.gov .